A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17427184



Internal ID22485054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:146240117..146240179hg38UCSC Ensembl
chr3:145957904..145957966hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5900693
Supporting Variants
Samples
Known GenesPLSCR4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17427184
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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